2,5-Dimethoxy-4-ethylthioamphetamine (CHEM132024)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-14 19:36:05 UTC | ||||||||
| Update Date | 2026-05-14 19:38:42 UTC | ||||||||
| Accession Number | CHEM132024 | ||||||||
| Identification | |||||||||
| Common Name | 2,5-Dimethoxy-4-ethylthioamphetamine | ||||||||
| Class | Small Molecule | ||||||||
| Description | 2,5-Dimethoxy-4-ethylthioamphetamine belongs to the phenethylamines, a subclass of benzene and substituted derivatives within the organic compounds. This benzenoid compound has the chemical formula C13H21NO2S and an average molecular weight of 255.38 g/mol. In terms of its pharmacological profile, two protein targets have been recorded for this substance. It acts as an agonist of 5-hydroxytryptamine receptor 2A (HTR2A) and 5-hydroxytryptamine receptor 2C (HTR2C). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C13H21NO2S | ||||||||
| Average Molecular Mass | 255.380 g/mol | ||||||||
| Monoisotopic Mass | 255.129 g/mol | ||||||||
| CAS Registry Number | 185562-00-9 | ||||||||
| IUPAC Name | 1-[4-(ethylsulfanyl)-2,5-dimethoxyphenyl]propan-2-amine | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | CCSC1=CC(OC)=C(CC(C)N)C=C1OC | ||||||||
| InChI Identifier | InChI=1S/C13H21NO2S/c1-5-17-13-8-11(15-3)10(6-9(2)14)7-12(13)16-4/h7-9H,5-6,14H2,1-4H3 | ||||||||
| InChI Key | MCYCODJKXUJSAT-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
